A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5799864



Internal ID8777267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85006839..85009573hg38UCSC Ensembl
chr16:85040445..85043179hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg382735
hg192735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660467
Supporting Variants
SamplesNA18487
Known GenesZDHHC7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5799864
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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